Canonical Allele Identifier: CA1457434235
Gene: SGCB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.52038299T= , CM000666.2:g.52038299T= GRCh38
NC_000004.11:g.52904465T= , CM000666.1:g.52904465T= GRCh37
NC_000004.10:g.52599222T= NCBI36
NG_008891.1:g.5021A= , LRG_204:g.5021A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381431.10:c.-40A= MANE Select ENSP00000370839.6:n.-40A=
ENST00000381431.9:c.-40A= ENSP00000370839.5:n.-40A=
NM_000232.4:c.-40A= , LRG_204t1:c.-40A= NP_000223.1:n.-40A=
NM_000232.5:c.-40A= MANE Select NP_000223.1:n.-40A=